Canonical Allele Identifier: PA645479829
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330000
ClinVar RCV Id: RCV000967625 RCV001764298 RCV002263049 RCV003912380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264055.1:p.Arg1031Gly
CA9638781
NM_001277126.2:c.3091C>G